Medicines for Malaria Venture COVID Box: a source for repurposing drugs with antifungal activity against human pathogenic fungi
Author(s) -
Rodrigo AlmeidaPaes,
Iara Bastos de Andrade,
Mariana Lucy Mesquita Ramos,
Marcus Rodrigues,
Vinícius Alves,
Andréa Reis BernardesEngemann,
Susana Frasés
Publication year - 2021
Publication title -
memórias do instituto oswaldo cruz
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.839
H-Index - 89
eISSN - 1678-8060
pISSN - 0074-0276
DOI - 10.1590/0074-02760210207
Subject(s) - cryptococcus neoformans , niclosamide , biology , fungicide , pharmacology , antifungal , paracoccidioides brasiliensis , microbiology and biotechnology , antifungal drugs , ecology , botany
BACKGROUND Treatment of mycoses is often ineffective, usually prolonged, and has some side effects. These facts highlight the importance of discovering new molecules to treat fungal infections. OBJECTIVES To search the Medicines for Malaria Venture COVID Box for drugs with antifungal activity. METHODS Fourteen human pathogenic fungi were tested against the 160 drugs of this collection at 1.0 µM concentration. We evaluated the ability of the drugs to impair fungal growth, their fungicidal nature, and morphological changes caused to cells. FINDINGS Thirty-four molecules (21.25%) presented antifungal activity. Seven are antifungal drugs and one is the agricultural fungicide cycloheximide. The other drugs with antifungal activity included antibiotics (n = 3), antimalarials (n = 4), antivirals (n = 2), antiparasitcs (n = 3), antitumor agents (n = 5), nervous system agents (n = 3), immunosuppressants (n = 3), antivomiting (n = 1), antiasthmatic (n = 1), and a genetic disorder agent (n = 1). Several of these drugs inhibited Histoplasma capsulatum and Paracoccidioides brasiliensis growth (15 and 20, respectively), while Fusarium solani was not affected by the drugs tested. Most drugs were fungistatic, but niclosamide presented fungicidal activity against the three dimorphic fungi tested. Cyclosporine affected morphology of Cryptococcus neoformans . MAIN CONCLUSIONS These drugs represent new alternatives to the development of more accessible and effective therapies to treat human fungal infections.
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